Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735683Generated: October 30, 2026

Triethylamine → HCID 56610267, compound

https://huagongshe.com/reaction/1735683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantChloroform methanol waterHCID 21866399—
ReactantHCID 53471022HCID 53471022—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 56610267HCID 56610267—

Reaction Steps

2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (BOC-ON) (121 mg, 0.49 mmole) (Aldrich Chem. Co., Milwaukee, Wis.) was added to a solution of S-(3-sulfopropyl)cysteine (SulfoCys, 100 mg, 0.41 mmole), (prepared by the method of U. T. Ruegg and J. Rudinger, J. Peptide Protein Res. 6, 447, 1974), and triethylamine (O.18 ml, 1.23 mmole) in 3 ml of 50% aqueous dioxane to form a reaction mixture. The reaction mixture was heated at 50°-55° C. for 1 hour to obtain a yellow solution. The reaction mixture was then cooled, diluted with 5 ml of water, and washed with ethylacetate (3×10 ml). The resultant aqueous layer was evaporated to dryness under vacuo by coevaporating with methanol twice. TLC (Silica gel 60, Merck & Co., Inc.) analysis of the residue produced by the evaporation, using a solvent system of chloroform/methanol/water (55:40:5), showed complete conversion of SulfoCys to BOC-SulfoCys.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538901
Source datasetuspto-grants-1996_07
ORD IDord-91f2d2e2213b415f8a39edc26ce2bda1
Source noteuspto-grants-1996_07